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Paritaprevir, ritonavir, ombitasvir, and dasabuvir with and without ribavirin in people with HCV genotype 1 and recent injecting drug use or receiving opioid substitution therapy
- Source :
- International Journal of Drug Policy. 62:94-103
- Publication Year :
- 2018
- Publisher :
- Elsevier BV, 2018.
-
Abstract
- Background: Direct-acting antiviral therapy for hepatitis C virus (HCV) infection is safe and effective, but there are little data among people who have recently injected drugs. This study evaluated the efficacy, and safety of paritaprevir/ritonavir, ombitasvir, dasabuvir with or without ribavirin for chronic HCV genotype (G) 1 among people with recent injecting drug use and/or receiving OST. Methods: D3FEAT is an international open-label study that recruited treatment-naive participants with recent injecting drug use (previous 6 months) and/or receiving OST with chronic HCV G1 infection between June 2016 and February 2017 in seven countries. Participants received paritaprevir/ritonavir, ombitasvir, dasabuvir with (G1a) or without ribavirin (G1b) administered twice daily in a one-week electronic blister pack (records timing of each dose) for 12 weeks. The primary endpoint was undetectable HCV RNA 12 weeks post-treatment (SVR12). Results: Among 87 participants (median age 48 years), 23% were female, 8% had cirrhosis, and 90% had G1a. Overall, 71% were receiving OST, 61% injected in the previous six months, 45% injected in the previous month, and 15% injected > daily. Treatment completion was 97% (84 of 87). There were no virological breakthroughs, but three discontinuations (loss to follow-up, n = 1; non-adherence, n = 1; incarceration, n = 1). SVR was 91% (79 of 87, 95% CI, 83%–96%). Five participants who completed treatment did not have SVR (loss to follow-up, n = 1; death, n = 1; virologic relapse, n = 3). Drug use prior to and during treatment did not impact SVR12. Treatment-related adverse events were observed in 46 (53%) patients (six grade 3, no grade 4). Five (6%) patients had at least one serious adverse event (two possibly/probably related to therapy; nausea and myoclonus). Two cases of reinfection were observed. Conclusion: Paritaprevir/ritonavir, ombitasvir, and dasabuvir with or without ribavirin for 12 weeks is effective among people with HCV genotype 1 with recent injecting drug use and/or receiving OST.
- Subjects :
- Cyclopropanes
Male
Sustained Virologic Response
Medicine (miscellaneous)
Hepacivirus
chemistry.chemical_compound
0302 clinical medicine
2-Naphthylamine
Anilides
030212 general & internal medicine
Substance Abuse, Intravenous
Qualitative Research
Sulfonamides
Dasabuvir
Health Policy
virus diseases
Valine
Hepatitis C
Middle Aged
Treatment Outcome
RNA, Viral
Drug Therapy, Combination
030211 gastroenterology & hepatology
medicine.symptom
medicine.drug
Adult
medicine.medical_specialty
Macrocyclic Compounds
Proline
Nausea
Lactams, Macrocyclic
Antiviral Agents
Drug Administration Schedule
Medication Adherence
03 medical and health sciences
Internal medicine
Ribavirin
Opiate Substitution Treatment
medicine
Humans
Uracil
Adverse effect
Ritonavir
business.industry
Hepatitis C, Chronic
medicine.disease
Ombitasvir
chemistry
Paritaprevir
Carbamates
business
Subjects
Details
- ISSN :
- 09553959
- Volume :
- 62
- Database :
- OpenAIRE
- Journal :
- International Journal of Drug Policy
- Accession number :
- edsair.doi.dedup.....91ed53cf823d3bc23d54c91273597287